Orphanet: Diagenom GmbH
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Diagenom GmbH

  • Diagenom GmbH
  • Robert-Koch-Str. 10
  • 18059 ROSTOCK
  • GERMANY
  • Status : Private for-profit
  • Phone : 49 (0)381 44022410
  • Additional Phone : -
  • Fax : 49 (0)381 44022419
  • Website
  • Contact
  • EUGT number : EUGTDE188899

Contacts

Quality management

Accreditation
 Accreditation

Accreditation
Organism
Year
Accreditation scope

EQA
 EQA

EQA scheme(s) organized by EMQN

11p-Imprinting Disorder Scheme (BWS/SRS)
2016, 2019
ADPKD (Adult dominant polycystic kidney disease)
2016, 2019
AZF (Y-Chromosome microdeletions)
2016, 2017, 2018
BRAF (Molecular testing for malignant melanoma)
2016, 2018
CAH (Congenital Adrenal Hyperplasia)
2016, 2017, 2018
CMT/HNPP (Charcot-Marie-Tooth disease / Hereditary Neuropathy with Pressure Palsies)
2016, 2019
Cardiac genetics - arrthymias
2019
DFNB1 (Hereditary Deafness)
2016, 2017, 2018
DM (Myotonic dystrophy)
2016
DMD (Duchenne and Becker muscular dystrophies)
2016, 2017, 2018
FAP (Familial Adenomatous Polyposis Colon Cancer)
2016, 2019
FH (Familial hypercholesterolemia - pilot scheme)
2016
FRDA (Friedreich ataxia)
2016
Germline NGS mutation testing
2016, 2017, 2018
HBOC (Hereditary Breast and Ovarian Cancer testing)
2016, 2017, 2018
HD (Huntington disease)
2016, 2017, 2018
HFE (Hereditary hemochromatosis)
2016
HNPCC (Hereditary non-polyposis colon cancer)
2016, 2017, 2018
HRF (Hereditary Recurrent Fevers)
2016, 2019
KRAS (Molecular testing for sporadic colorectal cancer)
2016, 2018
MEN2 (Multiple Endocrine Neoplasia Type 2)
2016
Molecular testing of germline changes in BRCA genes for ovarian cancer
2017, 2018
MonoDiab (Monogenic Diabetes)
2016, 2019
OI (Osteogenesis imperfecta)
2016, 2019
ONCOPANEL (Oncogene panel testing) - pilot scheme
2016, 2017, 2019
PKU (Phenylketonuria)
2016
POR (Porphyria)
2016
PWAS (Prader-Willi and Angelman syndromes)
2016, 2017, 2018
RYR1 related disorders
2019
SCA (Spinocerebellar ataxias)
2016, 2019
SEQ (DNA sequencing) - Full scheme
2016, 2017, 2018
SMA (Spinal muscular atrophy)
2016, 2017, 2018
Somatic NGS mutation testing
2018
Stickler syndrome
2019
VHL (Von Hippel Lindau syndrome)
2016, 2017
WIL (Wilson disease)
2016, 2017
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.